A Ketogenic Diet Sensitizes Pancreatic Cancer to Inhibition of Glutamine Metabolism

Author:

Hajihassani OmidORCID,Zarei Mehrdad,Roichman Asael,Loftus Alexander,Boutros Christina S.,Hue Jonathan,Naji Parnian,Boyer Jacob,Tahan Soubhi,Gallagher Peter,Beegan William,Choi James,Lei Shihong,Kim Christine,Rathore Moeez,Nakazzi Faith,Shah Ishan,Lebo Kevin,Cheng Helen,Mudigonda Anusha,Alibeckoff Sydney,Ji Karen,Graor Hallie,Miyagi Masaru,Vaziri-Gohar Ali,Brunengraber Henri,Wang RuiORCID,Lund Peder J.ORCID,Rothermel Luke D.,Rabinowitz Joshua D.,Winter Jordan M.

Abstract

AbstractPancreatic cancer is the third leading cause of cancer death in the United States, and while conventional chemotherapy remains the standard treatment, responses are poor. Safe and alternative therapeutic strategies are urgently needed1. A ketogenic diet has been shown to have anti-tumor effects across diverse cancer types but will unlikely have a significant effect alone. However, the diet shifts metabolism in tumors to create new vulnerabilities that can be targeted (1). Modulators of glutamine metabolism have shown promise in pre-clinical models but have failed to have a marked impact against cancer in the clinic. We show that a ketogenic diet increases TCA and glutamine-associated metabolites in murine pancreatic cancer models and under metabolic conditions that simulate a ketogenic dietin vitro.The metabolic shift leads to increased reliance on glutamine-mediated anaplerosis to compensate for low glucose abundance associated with a ketogenic diet. As a result, glutamine metabolism inhibitors, such as DON and CB839 in combination with a ketogenic diet had robust anti-cancer effects. These findings provide rationale to study the use of a ketogenic diet with glutamine targeted therapies in a clinical context.Graphical AbstractGraphical Abstract Description:Mechanistic rationale for combining a ketogenic diet and glutamine metabolism inhibitors.The combination of low glucose from a ketogenic diet and pharmacologic glutamine inhibition impairs nutrient input to mitochondria, reducing cancer growth.

Publisher

Cold Spring Harbor Laboratory

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